Singclean Flu a/B Antigen Test Kit Rapid AG Diagnostic CE Approved

Influenza a/B Rapid Test Kit, AG Test, Antibody Test Strip CE/White List

INTENDED USE

FLU A/B Antigen Test Kit (Colloidal Gold) is used for in vitro qualitative detection of influenza A/B antigen in human nasopharyngeal swab samples

PACK FORMATS

1 Test/Box

10 Tests/Box

20 Tests/Box

50 Tests/Box

INTRODUCTION

Influenza viruses (Flu) are the pathogens that cause influenza. Influenza is an acute respiratory infection caused by influenza A, B, and C viruses. It is infectious strong, fast spread, short incubation period, high incidence. Influenza A virus often appears in epidemic form and can cause a worldwide influenza pandemic. It is widely distributed in animals and can also cause influenza epidemics in animals and cause a large number of animal deaths. Influenza B virus often causes local outbreaks and does not cause a worldwide influenza pandemic. Therefore, the detection of influenza A and B viruses has relatively great clinical findings.

MATERIALS SUPPLIED

1. Test Cassette

2. Sampling cotton swabs (as nasopharyngeal swab)

3. Antigen extraction buffer

4. Antigen extraction tube

5. Paper workbench(The small one-test-box can be used as a workbench)

6. Instruction for use

STORAGE AND STABILITY

The kit can be stored at 4-30°C. The test device is stable through the expiration date printed on the sealed pouch. The test device must remain in the sealed pouch until use.

Do not freeze. Do not use beyond the expiration date. After opening the sealed pouch, use the test as soon as possible within 60 minutes.
 

SPECIMEN COLLECTION

1. FLU A/B Antigen Test kit(Colloidal Gold)can be performed using nasopharyngeal swab.

2. Testing should be performed immediately after specimen collection.

3. Bring specimens to room temperature prior to testing.

4. If specimens are to be shipped, they should be packed in compliance with local regulations covering the transportation of etiologic agents.
 

TEST PROCEDURE

Allow test cassette, Antigen extraction buffer, specimen and/or controls to equilibrate to room temperature prior to testing.

1. Ask the patient to remove the secretions on the surface of the anterior nasal cavity, keep the head slightly tilted, and gently and slowly insert the swab through the nasal cavity to the nasopharynx, When resistance is encountered, it will reach the posterior nasopharynx, stay for a few seconds to absorb secretions, and gently rotate to remove the swab.

2. Place the antigen extraction tube on the workbench. Place the antigen extraction buffer bottle vertically downward, squeeze the bottle to make the buffer drip freely into the antigen extraction tube without touching the edge of the tube, and add 6 drops (about 200ul) to the antigen extraction tube.

3. Put the swab specimen into the antigen extraction tube pre-added with the antigen extraction buffer, and rotate the swab about 10 times while pressing the swab head against the tube wall to release the antigen in the swab, then let it stand for about 1 minute.

4. Remove the swab while squeezing the tip of the swab so that as much liquid in the swab can be discharged as possible. Dispose of used swabs in accordance with biohazard waste disposal methods.

5. Install the dripper on the antigen extraction tube and cap it tightly, and let it stand for about 1 minute.

6. Remove the test cassette from the sealed foil pouch and use it as soon as possible.

7. Place the test device on a clean and level surface.

8. Transfer 3 drops(about 100ul) of mix Liquids to the sample well of the test card (or use a pipette to add 100ul), and start the timer.

9. Wait for the test result of the reagent. The result should be read in 15 minutes. Do not interpret the result after 20 minutes.

 

INTERPRETATION OF RESULTS

NEGATIVE:

If only the C band is present, the absence of any burgundy color in the T band indicates that no FLU A/B antigens are detected in the specimen. The result is negative.

POSITIVE

FLU A/B positive:

In addition to the presence of the C-line, If the test lines A and B appears at the same time, it means that there are both influenza A virus antigen and influenza B virus antigen in the sample, that is, the result is positive for FLU A and FLU B.

FLU A positive:

In addition to the presence of the C-line, if the test line A appears, the test indicates the presence of FLU A antigen in the sample, that is, the result is positive for FLU A.

FLU B positive:

In addition to the presence of the C-line, if the test line B appears, the test indicates the presence of FLU B antigen in the sample, that is, the result is positive for FLU B.

INVALID:

Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test cassette.

If the problem persists, discontinue using the test kit immediately and contact your local distributor.

 

LIMITATIONS

1. Use fresh samples whenever possible.

2. Optimal assay performance requires strictly adherence to the assay procedure described in Instruction for use. Deviations may lead to aberrant results.

3. A negative result for an individual subject indicates absence of detectable FLU A/B antigen. However, a negative test result does not preclude the possibility of exposure to or infection with FLU A/B.

4. A negative result can occur if the quantity of the FLU A/B antigen present in the specimen is below the detection limits of the assay, or failed to collect the FLU A/B antigen in the nasal cavity of the patient.

5. As with all diagnostic tests, a definitive clinical diagnosis should not be based on the result of a single test, but should only be made by the physician after all clinical and laboratory findings have been evaluated.